噻二唑的合成方法、化学和抗惊厥活性。

International Journal of Medicinal Chemistry Pub Date : 2013-01-01 Epub Date: 2013-04-30 DOI:10.1155/2013/348948
Bhawna Sharma, Amita Verma, Sunil Prajapati, Upendra Kumar Sharma
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引用次数: 51

摘要

长期以来,杂环化合物的化学研究一直是一个有趣的研究领域。杂环核1,3,4-噻二唑是一类重要的新药开发化合物。近几十年来,新型噻二唑衍生物的合成及其化学和生物学行为的研究日益受到重视。寻找具有更强选择性活性和更低毒性的抗癫痫化合物一直是药物化学研究的一个活跃领域。近年来,人们对不同类别的噻二唑类化合物进行了广泛的研究,其中许多化合物具有广泛的药理活性,即抗菌活性、抗惊厥活性、抗真菌活性、抗糖尿病活性、抗炎活性、抗氧化活性和抗结核活性等。对现有药物的耐药性正迅速成为一个世界性的主要问题。需要设计新的化合物来处理这种抗性已成为当今最重要的研究领域之一。噻二唑是一种具有多种生物活性的多用途基团。噻二唑部分作为“氢结合域”和“双电子供体系统”。它也作为一个受约束的药效团。本文在文献报道的基础上,对噻二唑类化合物及其合成方法、化学性质和抗惊厥活性进行了研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Synthetic methods, chemistry, and the anticonvulsant activity of thiadiazoles.

Synthetic methods, chemistry, and the anticonvulsant activity of thiadiazoles.

Synthetic methods, chemistry, and the anticonvulsant activity of thiadiazoles.

Synthetic methods, chemistry, and the anticonvulsant activity of thiadiazoles.

The chemistry of heterocyclic compounds has been an interesting field of study for a long time. Heterocyclic nucleus 1,3,4-thiadiazole constitutes an important class of compounds for new drug development. The synthesis of novel thiadiazole derivatives and investigation of their chemical and biological behavior have gained more importance in recent decades. The search for antiepileptic compounds with more selective activity and lower toxicity continues to be an active area of intensive investigation in medicinal chemistry. During the recent years, there has been intense investigation of different classes of thiadiazole compounds, many of which possess extensive pharmacological activities, namely, antimicrobial activity, anticonvulsant, antifungal antidiabetic, anti-inflammatory, antioxidant, and antituberculosis activities, and so forth. The resistance towards available drugs is rapidly becoming a major worldwide problem. The need to design new compounds to deal with this resistance has become one of the most important areas of research today. Thiadiazole is a versatile moiety that exhibits a wide variety of biological activities. Thiadiazole moiety acts as "hydrogen binding domain" and "two-electron donor system." It also acts as a constrained pharmacophore. On the basis of the reported literature, we study here thiadiazole compounds and their synthetic methods chemistry and anticonvulsant activity.

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期刊介绍: International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis. International Journal of Medicinal Chemistry is a peer-reviewed, Open Access journal that publishes original research articles as well as review articles in all areas of chemistry associated with drug discovery, design, and synthesis.
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